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Ampicillin

NDC 71872-7332 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, FOR SOLUTION

Labeler / ManufacturerMedical Purchasing Solutions, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA201025
Dosage form / routeINJECTION, POWDER, FOR SOLUTION · INTRAMUSCULAR INTRAVENOUS
Active ingredientsAMPICILLIN SODIUM (1 g/1)
Marketing started20231110
Package count1

External sources

Source: openFDA. Public-domain (CC0).